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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096582copy number variation2nstd102humanUncertain significance GRCh37 chr2: 169,853,125-170,344,644 , GRCh38.p12 chr2: 168,996,615-169,488,134 DHRS9, ABCB11, 3 more genes
    nsv7052314inversion1nstd229human GRCh38 chr2: 169,082,906-169,105,200 , GRCh37.p13 chr2: 169,939,416-169,961,710 DHRS9
    nsv7043143inversion1nstd229human GRCh38 chr2: 169,066,388-169,066,488 , GRCh37.p13 chr2: 169,922,898-169,922,998 DHRS9
    nsv7041452inversion1nstd229human GRCh38 chr2: 169,071,834-169,088,596 , GRCh37.p13 chr2: 169,928,344-169,945,106 DHRS9
    nsv6698060copy number variation1nstd229human GRCh38 chr2: 168,845,584-169,182,309 , GRCh37.p13 chr2: 169,702,094-170,038,819 LRP2, ABCB11, 5 more genes
    nsv6689371copy number variation1nstd229human GRCh38 chr2: 169,067,401-169,074,900 , GRCh37.p13 chr2: 169,923,911-169,931,410 DHRS9
    nsv6685624copy number variation1nstd229human GRCh38 chr2: 169,082,130-169,207,374 , GRCh37.p13 chr2: 169,938,640-170,063,884 DHRS9, LRP2, 1 more genes
    nsv6682110copy number variation1nstd229human GRCh38 chr2: 169,043,765-169,080,980 , GRCh37.p13 chr2: 169,900,275-169,937,490 DHRS9
    nsv6681997copy number variation1nstd229human GRCh38 chr2: 169,094,801-169,105,200 , GRCh37.p13 chr2: 169,951,311-169,961,710 DHRS9
    nsv6681896copy number variation1nstd229human GRCh38 chr2: 169,073,054-169,081,354 , GRCh37.p13 chr2: 169,929,564-169,937,864 DHRS9
    nsv6680554copy number variation1nstd229human GRCh38 chr2: 169,094,936-169,106,262 , GRCh37.p13 chr2: 169,951,446-169,962,772 DHRS9
    nsv6679475copy number variation1nstd229human GRCh38 chr2: 169,091,270-169,091,301 , GRCh37.p13 chr2: 169,947,780-169,947,811 DHRS9
    nsv6678900copy number variation1nstd229human GRCh38 chr2: 168,515,191-170,305,528 , GRCh37.p13 chr2: 169,371,701-171,162,038 METTL5, FASTKD1, 28 more genes
    nsv6627781copy number variation1nstd224human GRCh37 chr2: 168,698,913-170,141,066 , GRCh38.p12 chr2: 167,842,403-169,284,556 STK39, CERS6, 17 more genes
    nsv6627281copy number variation1nstd224human GRCh37 chr2: 169,668,122-169,927,200 , GRCh38.p12 chr2: 168,811,612-169,070,690 G6PC2, ABCB11, 3 more genes
    nsv6550789inversion1nstd223human GRCh38 chr2: 169,079,138-169,079,823 , GRCh37.p13 chr2: 169,935,648-169,936,333 DHRS9
    nsv6545572inversion1nstd223human GRCh38 chr2: 169,071,834-169,088,594 , GRCh37.p13 chr2: 169,928,344-169,945,104 DHRS9
    nsv6353054copy number variation1nstd223human GRCh38 chr2: 169,066,961-169,067,629 , GRCh37.p13 chr2: 169,923,471-169,924,139 DHRS9
    nsv6351791copy number variation1nstd223human GRCh38 chr2: 169,070,796-169,082,305 , GRCh37.p13 chr2: 169,927,306-169,938,815 DHRS9
    nsv6343431copy number variation1nstd223human GRCh38 chr2: 169,071,374-169,071,783 , GRCh37.p13 chr2: 169,927,884-169,928,293 DHRS9
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